NDC 72127-0702 - Forticept Blue Butter Antimicrobial Gel

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
72127-0702
Package NDCs from labels
72127-0702-4, 72127-0702-8, 72127-0702-2
Manufacturer
Lidan, Inc. | Cosco International, Inc.
Effective date
2023-01-13
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Forticept Blue Butter Antimicrobial GelLidan, Inc. | Cosco International, Inc.2023-01-13OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72127-0702-2Forticept Blue Butter Antimicrobial Gel60 g in 1 TUBEGel604
72127-0702-4Forticept Blue Butter Antimicrobial Gel114 g in 1 CANGel1144
72127-0702-8Forticept Blue Butter Antimicrobial Gel240 g in 1 CANGel2404

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72127-0702FORTICEPT BLUE BUTTER ANTIMICROBIAL GEL (BENZETHONIUM CHLORIDE, THYMOL) GEL [LIDAN, INC.]43 package rows20230115_87fb4c7e-1d7d-4823-b0f2-dc756c7e5492.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 14 of 14 · 262 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
CPAP Mask cleaning wipesBENZETHONIUM CHLORIDE AND BENZALKONIUM CHLORIDEJIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD.412e6fec-5af5-45f7-8c6b-393b884e161c2019-06-07WarningsExact identifier
unii: PH41D05744
Hand WipesCHLORHEXIDINE DIGLUCONATE AND BENZETHONIUM CHLORIDEJIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD.181e5fa0-ddda-4783-a0b5-ff95bfce6b362017-10-09WarningsExact identifier
unii: PH41D05744

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.